AB032. Mutation spectrum in the dystrophin gene disclosed by multiplex ligation-dependent probe amplification in 181 Vietnamese Duchenne/Becker muscular dystrophy patients

Duchenne/Becker muscular dystrophy (DMD/BMD) the most common X-linked muscular dystrophy is caused by mutation in dystrophin gene. Deletion and duplication in the dystrophin gene account for 60-70% of mutation. Multiplex ligation-dependent probe amplification (MLPA) is the most powerful and convenie...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Ann Transl Med
Päätekijät: Tran, Van Khanh, Do, Ngoc Hai, Tran, Thinh Huy, Ta, Minh Hieu, Tuan-Pham, Le Anh, Chi, Dung Vu, Khanh, Nguyen Ngoc, Ta, Van Thanh, Matsuo, Masafumi
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: AME Publishing Company 2015
Aiheet:
Part 2: Symposium
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC4563477/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3978/j.issn.2305-5839.2015.AB032
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